Histological studies of the effects of chronic implantation of ceramic-based microelectrode arrays and microdialysis probes in rat prefrontal cortex.
Histological studies of the effects of chronic implantation of ceramic-based microelectrode arrays and microdialysis probes in rat prefrontal cortex.
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DOI:
10.1016/j.brainres.2009.06.084
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发表时间:
2009-09-29
期刊:
影响因子:
2.9
通讯作者:
Gerhardt GA
中科院分区:
文献类型:
--
作者:
Hascup ER;af Bjerkén S;Hascup KN;Pomerleau F;Huettl P;Strömberg I;Gerhardt GA
Chronic implantation of neurotransmitter measuring devices is essential for awake, behavioral studies occurring over multiple days. Little is known regarding the effects of long term implantation on surrounding brain parenchyma and the resulting alterations in the functional properties of this tissue. We examined the extent of tissue damage produced by chronic implantation of either ceramic microelectrode arrays (MEAs) or microdialysis probes. Histological studies were carried out on fixed tissues using stains for neurons (cresyl violet), astrocytes (GFAP), microglia (Iba-1), glutamatergic nerve fibers (VGLUT1), and the blood-brain barrier (SMI-71). Nissl staining showed pronounced tissue body loss with microdialysis implants compared to MEAs. The MEAs produced mild gliosis extending 50–100 µm from the tracks, with a significant change in the affected areas starting at 3 days. By contrast, the microdialysis probes produced gliosis extending 200–300 µm from the track, which was significant at 3 and 7 days. Markers for microglia and glutamatergic fibers supported that the MEAs produce minimal damage with significant changes occurring only at 3 and 7 days that return to control levels by one month. SMI-71 staining supported integrity of the blood brain barrier out to 1 week for both the microdialysis probes and the MEAs. This data support that the ceramic MEAs small size and biocompatibility are necessary to accurately measure neurotransmitter levels in the intact brain. The minimal invasiveness of the MEAs reduce tissue loss, allowing for long term (>6 month) electrochemical and electrophysiological monitoring of brain activity.
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影响因子:
3.4
作者:
Joyce, B. Matthew;Glaser, Paul E. A.;Gerhardt, Greg A.
通讯作者:
Gerhardt, Greg A.
DOI:
10.1006/bbrc.1996.1112
发表时间:
1996-07-25
影响因子:
3.1
作者:
Imai, Y;Ibata, I;Kohsaka, S
通讯作者:
Kohsaka, S
影响因子:
3
作者:
Borland, LM;Shi, GY;Michael, AC
通讯作者:
Michael, AC
影响因子:
3.7
作者:
BOURDELAIS, AJ;DEUTCH, AY
通讯作者:
DEUTCH, AY
影响因子:
12.6
作者:
Burmeister, JJ;Palmer, M;Gerhardt, GA
通讯作者:
Gerhardt, GA